Whipple's disease (patient information): Difference between revisions
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==Overview== | ==Overview== | ||
Whipple's disease is a rare condition that prevents the intestine from properly absorbing nutrients. This is called malabsorption. | Whipple's disease is a rare condition that prevents the [[intestine]] from properly absorbing [[nutrients]]. This is called [[malabsorption]]. | ||
==What are the symptoms of Whipple's disease?== | ==What are the symptoms of Whipple's disease?== | ||
Symptoms usually start slowly. Joint | Symptoms usually start slowly. [[Joint pain]] is the most common initial symptom. After that, often several years later, symptoms of [[gastrointestinal]] infection develop. Other symptoms may include: | ||
*[[Abdominal pain]] | *[[Abdominal pain]] | ||
| Line 14: | Line 14: | ||
*[[Fever]] | *[[Fever]] | ||
*Gray to brown skin color | *Gray to brown skin color | ||
*Joint pain | *[[Joint pain]] in the [[Ankle|ankles]], [[knees]], [[elbows]], [[fingers]], or other areas | ||
*[[Memory loss]] | *[[Memory loss]] | ||
* | *[[Personality changes]] | ||
*[[Weight loss]] | *[[Weight loss]] | ||
==What causes Whipple's disease?== | ==What causes Whipple's disease?== | ||
Whipple's disease is caused by bacteria named Tropheryma | Whipple's disease is caused by bacteria named [[Tropheryma whipplei]]. It can affect any system of the body, but occurs most often in the [[small intestine]]. [[Lesions]] appear on the wall of the [[small intestine]] and thicken the tissue. The [[villi]]—tiny, finger-like protrusions from the wall that help absorb [[nutrients]]—are damaged. | ||
==Who is at highest risk?== | ==Who is at highest risk?== | ||
Although risk factors for Whipple's disease are unknown the disorder mainly affects middle-aged white men. | Although risk factors for Whipple's disease are unknown, the disorder mainly affects middle-aged white men. | ||
==Diagnosis== | ==Diagnosis== | ||
'''Possible signs:''' | '''Possible signs:''' | ||
* Enlarged lymph | * Enlarged [[lymph nodes]] | ||
* Fatty stools | * [[Fatty stools]] | ||
* Gastrointestinal bleeding | * [[Gastrointestinal bleeding]] | ||
* Swelling in body tissues (edema) | * [[Swelling]] in body tissues ([[edema]]) | ||
'''Tests may include:''' | '''Tests may include:''' | ||
*[[Complete blood count]] | *[[Complete blood count]] | ||
*[[Polymerase chain reaction]] (PCR) test to check for the bacteria that causes the disease | *[[Polymerase chain reaction]] ([[PCR]]) test to check for the [[bacteria]] that causes the disease | ||
*[[Small bowel biopsy]] | *[[Small bowel]] [[biopsy]] | ||
*Upper GI endoscopy (viewing the intestines with a flexible, lighted tube in a process called [[enteroscopy]]) | *[[Endoscopy|Upper GI endoscopy]] (viewing the intestines with a flexible, lighted tube in a process called [[enteroscopy]]) | ||
'''This disease may also change the results of the following tests:''' | '''This disease may also change the results of the following tests:''' | ||
* Albumin | * [[Albumin]] | ||
* Unabsorbed fat in the stools (fecal fat) | * Unabsorbed fat in the stools ([[fecal fat]]) | ||
* Intestinal absorption of a type of sugar (d-xylose absorption) | * [[Intestinal]] [[absorption]] of a type of sugar ([[d-xylose]] absorption) | ||
==When to seek urgent medical care?== | ==When to seek urgent medical care?== | ||
Call your health care provider if you have persistent abdominal pain and diarrhea. | Call your health care provider if you have persistent [[abdominal pain]] and [[diarrhea]]. | ||
If you are being treated for Whipple's disease, call your | If you are being treated for Whipple's disease, call your healthcare provider if: | ||
* Symptoms worsen or do not improve | * Symptoms worsen or do not improve | ||
* Symptoms reappear | * Symptoms reappear | ||
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==Treatment options== | ==Treatment options== | ||
You will need to take long-term antibiotics to cure any infections of the brain and central nervous system. A medicine called ceftriaxone is given through a vein | You will need to take long-term [[antibiotics]] to cure any [[infections]] of the [[brain]] and [[central nervous system]]. A medicine called [[ceftriaxone]] is given through a [[vein]]. It is followed by an [[antibiotic]] (such as [[Sulfamethoxazole-Trimethoprim|trimethoprim-sulfamethoxazole]]) taken by mouth for up to 1 year. | ||
If symptoms come back during antibiotic use, the antibiotic treatment may be changed. | If symptoms come back during [[antibiotic]] use, the [[antibiotic]] treatment may be changed. | ||
Your | Your healthcare provider should closely follow you, because signs of the disease can return after you finish therapy. Those who have [[nutritional deficiencies]] from [[malabsorption]] will also need to take [[dietary supplements]]. | ||
Depending on the seriousness of the disease, treatment may also include fluid and electrolyte replacement. Electrolytes are salts and other substances in body fluid that the heart and brain need to function properly. Extra iron, folate, vitamin D, calcium, and magnesium may also be given to help compensate for the vitamins and minerals the body cannot absorb on its own. | Depending on the seriousness of the disease, treatment may also include fluid and [[electrolyte]] replacement. [[Electrolyte|Electrolytes]] are [[salts]] and other substances in [[body fluid]] that the [[heart]] and [[brain]] need to function properly. Extra [[iron]], [[folate]], [[vitamin D]], [[calcium]], and [[magnesium]] may also be given to help compensate for the [[vitamins]] and [[minerals]] the body cannot absorb on its own. | ||
==Where to find medical care for Whipple's disease?== | ==Where to find medical care for Whipple's disease?== | ||
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*[[Brain damage]] | *[[Brain damage]] | ||
*[[Heart valve]] damage (from [[endocarditis]]) | *[[Heart valve]] damage (from [[endocarditis]]) | ||
*Nutritional deficiencies | *[[Nutritional deficiencies]] | ||
*[[Weight loss]] | |||
*Symptoms return (which may be because of drug resistance) | *Symptoms return (which may be because of drug resistance) | ||
==Sources== | ==Sources== | ||
Revision as of 01:47, 3 November 2017
For the WikiDoc page for this topic, click here
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Whipple's disease |
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Whipple's disease On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Assistant Editor-in-Chief: Meagan E. Doherty
Overview
Whipple's disease is a rare condition that prevents the intestine from properly absorbing nutrients. This is called malabsorption.
What are the symptoms of Whipple's disease?
Symptoms usually start slowly. Joint pain is the most common initial symptom. After that, often several years later, symptoms of gastrointestinal infection develop. Other symptoms may include:
- Abdominal pain
- Diarrhea
- Fever
- Gray to brown skin color
- Joint pain in the ankles, knees, elbows, fingers, or other areas
- Memory loss
- Personality changes
- Weight loss
What causes Whipple's disease?
Whipple's disease is caused by bacteria named Tropheryma whipplei. It can affect any system of the body, but occurs most often in the small intestine. Lesions appear on the wall of the small intestine and thicken the tissue. The villi—tiny, finger-like protrusions from the wall that help absorb nutrients—are damaged.
Who is at highest risk?
Although risk factors for Whipple's disease are unknown, the disorder mainly affects middle-aged white men.
Diagnosis
Possible signs:
- Enlarged lymph nodes
- Fatty stools
- Gastrointestinal bleeding
- Swelling in body tissues (edema)
Tests may include:
- Complete blood count
- Polymerase chain reaction (PCR) test to check for the bacteria that causes the disease
- Small bowel biopsy
- Upper GI endoscopy (viewing the intestines with a flexible, lighted tube in a process called enteroscopy)
This disease may also change the results of the following tests:
- Albumin
- Unabsorbed fat in the stools (fecal fat)
- Intestinal absorption of a type of sugar (d-xylose absorption)
When to seek urgent medical care?
Call your health care provider if you have persistent abdominal pain and diarrhea.
If you are being treated for Whipple's disease, call your healthcare provider if:
- Symptoms worsen or do not improve
- Symptoms reappear
- New symptoms develop
Treatment options
You will need to take long-term antibiotics to cure any infections of the brain and central nervous system. A medicine called ceftriaxone is given through a vein. It is followed by an antibiotic (such as trimethoprim-sulfamethoxazole) taken by mouth for up to 1 year.
If symptoms come back during antibiotic use, the antibiotic treatment may be changed.
Your healthcare provider should closely follow you, because signs of the disease can return after you finish therapy. Those who have nutritional deficiencies from malabsorption will also need to take dietary supplements.
Depending on the seriousness of the disease, treatment may also include fluid and electrolyte replacement. Electrolytes are salts and other substances in body fluid that the heart and brain need to function properly. Extra iron, folate, vitamin D, calcium, and magnesium may also be given to help compensate for the vitamins and minerals the body cannot absorb on its own.
Where to find medical care for Whipple's disease?
Directions to Hospitals Treating Whipple's disease
What to expect (Outlook/Prognosis)
Without treatment, the condition is usually fatal. Treatment relieves symptoms and can cure the disease.
Possible Complications
- Brain damage
- Heart valve damage (from endocarditis)
- Nutritional deficiencies
- Weight loss
- Symptoms return (which may be because of drug resistance)
Sources
- http://digestive.niddk.nih.gov/ddiseases/pubs/whipple/index.htm
- http://www.nlm.nih.gov/medlineplus/ency/article/000209.htm